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Lack of Short-term Cancer Risk With Tainted Valsartan ‘Reassuring’

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Lack of Short-term Cancer Risk With Tainted Valsartan ‘Reassuring’

September 13, 2018

CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

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CV Devices in the Fast Lane: FDA’s Approval Often Rests on Early Evidence

September 05, 2018

TCTMD’s Top 10 Most Popular Stories for August 2018

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for August 2018

September 04, 2018

Valsartan Recall Expanded by FDA and European Medicines Agency

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Valsartan Recall Expanded by FDA and European Medicines Agency

August 10, 2018

TCTMD’s Top 10 Most Popular Stories for July 2018

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TCTMD’s Top 10 Most Popular Stories for July 2018

August 01, 2018

Sentinel Cerebral Embolic Protection Device Acquired by Boston Scientific

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Sentinel Cerebral Embolic Protection Device Acquired by Boston Scientific

July 20, 2018

High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

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High-Risk Medical Device Approval Process in Europe Inches Towards Transparency

Michael O'Riordan

July 20, 2018

FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

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FDA Recalls Valsartan-Containing Drugs After Detection of Carcinogen

Michael O'Riordan

July 16, 2018

FDA Advisory Panel Gives Thumbs Up to EVAR System

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FDA Advisory Panel Gives Thumbs Up to EVAR System

June 14, 2018

FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’

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FDA: Class I Recall for Cardiosave Hybrid IABP Due to ‘Fluid Ingress’

June 07, 2018

Class I Recall for Medtronic’s HeartWare HVAD System

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Class I Recall for Medtronic’s HeartWare HVAD System

Michael O'Riordan

June 04, 2018

News Industry News

FDA Classifies HeartWare(TM) HVAD(TM) Systems Unexpected Power Source Switching as Class I Recall

June 04, 2018

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HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA

May 23, 2018

HRS: Here’s How to Talk About Cybersecurity Concerns and Implantable Devices

News Conference News HRS 2018

HRS: Here’s How to Talk About Cybersecurity Concerns and Implantable Devices

May 17, 2018

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

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FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

April 20, 2018

Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

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Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs

February 27, 2018

FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

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FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks

Michael O'Riordan

January 17, 2018

Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

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Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

January 11, 2018

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FDA Posts Outdated Alert for Sapien 3 Transapical Delivery System

January 11, 2018

The Biggest News of 2017: TCTMD’s Top 10

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The Biggest News of 2017: TCTMD’s Top 10

January 01, 2018

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